Diagnosis of Variceal Bleeding and Its Control in Cirrhosis

Status

Terminated

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00188097

Enrollment

400

Registered

2005-09-16

Start date

1999-11-30

Completion date

2002-06-30

Last updated

2006-01-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cirrhosis

Brief summary

The aim of the study was to determine the independent predictors of variceal bleeding and control of bleeding in cirrhosis as no scientific assessment have been perfomed until now

Interventions

BEHAVIORALDiagnosis of variceal bleeding and dits control in cirrhosis

Study design

Allocation

NON_RANDOMIZED

Intervention model

SINGLE_GROUP

Primary purpose

PREVENTION

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to 75 Years

Healthy volunteers

Inclusion criteria

* Cirrhotic patients admitted for an acute complication of cirrhosis * admission ≤ 6 hours of inclusion

Exclusion criteria

* Child-Pugh score \> 13 * Digestive hemorrhage * Non cirrhotic portal hypertension

Design outcomes

Primary

Measure	Time frame
variceal bleeding	—

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026